Dermatomyositis-like Eruption Induced by Hydroxyurea-Case Report and Literature Review
- PMID: 40217643
- PMCID: PMC11990037
- DOI: 10.3390/jcm14072192
Dermatomyositis-like Eruption Induced by Hydroxyurea-Case Report and Literature Review
Abstract
Background: Hydroxyurea (HU) is a widely used chemotherapeutic agent for myeloproliferative disorders, yet its long-term use can rarely trigger a dermatomyositis-like (DM-like) eruption characterized solely by cutaneous manifestations without muscle involvement or serologic markers. This study presents a case of HU-induced DM-like eruption and reviews the literature regarding this rare occurrence. Methods: A 77-year-old woman with polycythemia vera on long-term HU therapy developed a progressively worsening, erythematous, scaly, and crusted eruption on the face, neck, and anterior thorax. Comprehensive clinical evaluations, laboratory tests (including normal muscle enzymes and negative autoimmune panels), and skin biopsies were performed. In parallel, a systematic literature review was conducted using databases such as PubMed, Scopus, and Google Scholar, incorporating case reports and series published prior to January 2025 that provided detailed individual clinical data. Results: The patient exhibited hallmark DM-like cutaneous features-interface dermatitis with basal vacuolar degeneration and prominent dermal mucin deposition-without evidence of muscle weakness or positive myositis-specific antibodies. The literature review of 23 cases revealed a median latency of 5 years from HU initiation to skin eruption, with the dorsal hands most frequently affected. HU discontinuation, often combined with systemic and topical corticosteroids (and, in some cases, steroid-sparing agents), resulted in lesion resolution in over 90% of cases, with a median healing time of approximately 3 months. Conclusions: HU-induced DM-like eruption, though infrequent, is a distinct clinical entity requiring prompt recognition and management. The main treatment is the discontinuation of HU, which, when supplemented by appropriate corticosteroid therapy, leads to significant clinical improvement. Ongoing dermatologic surveillance is recommended for patients on long-term HU therapy due to the potential risk of premalignant skin changes.
Keywords: adverse effect; dermatomyositis; hydroxyurea.
Conflict of interest statement
The authors declare no conflicts of interest.
Figures


Similar articles
-
Dermatomyositis-like eruption after long-term hydroxyurea therapy for polycythemia vera.Eur J Dermatol. 2002 Nov-Dec;12(6):586-8. Eur J Dermatol. 2002. PMID: 12459535
-
Hydroxyurea induced dermatomyositis-like eruption.Australas J Dermatol. 2012 Aug;53(3):e58-60. doi: 10.1111/j.1440-0960.2011.00774.x. Epub 2011 May 31. Australas J Dermatol. 2012. PMID: 22881475 Review.
-
Dermatomyositis-like Eruptions, Hydroxyurea-Associated Squamous Dysplasia, and Nonmelanoma Skin Cancer: A Case Report and Systematic Review.Dermatopathology (Basel). 2025 Mar 30;12(2):11. doi: 10.3390/dermatopathology12020011. Dermatopathology (Basel). 2025. PMID: 40265342 Free PMC article. Review.
-
Paraneoplastic Dermatomyositis in a Patient with Metastatic Gastric Carcinoma.Acta Dermatovenerol Croat. 2020 Aug;28(2):120-122. Acta Dermatovenerol Croat. 2020. PMID: 32876041
-
Dermatomyositis associated with omalizumab therapy for severe asthma: a case report.Allergy Asthma Clin Immunol. 2019 Jan 17;15:4. doi: 10.1186/s13223-019-0319-4. eCollection 2019. Allergy Asthma Clin Immunol. 2019. PMID: 30675173 Free PMC article.
References
-
- Yarbro J.W. Mechanism of action of hydroxyurea. Semin. Oncol. 1992;19((Suppl. 9)):1–10. - PubMed
Publication types
LinkOut - more resources
Full Text Sources